FDA inspection
Lacrimedics Inc: FDA inspection ending Mar 15, 2016
FDA inspection 966842 · Voluntary Action Indicated (VAI) · Dupont, WA
Key facts
| Inspection ID | 966842 |
|---|---|
| Firm | Lacrimedics Inc |
| FEI number | 2024818 |
| Address | 2620 Williamson Pl Ste 113 |
| City | Dupont |
| State | WA |
| ZIP | 98327 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Mar 15, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data